Issue 22, 2011

Expanded redox accessibility vialigand substitution in an octahedral Fe6Br6 cluster

Abstract

Oxidation of the nominally all-ferrous hexanuclear cluster (HL)2Fe6 with six equivalents of ferrocenium in the presence of bromide ions results in a six-electron oxidation of the Fe6 core to afford the nominally all-ferric cluster (HL)2Fe6Br6. The hexabromide cluster is also structurally characterized in a 4+ core oxidation state. A structural comparison of these two clusters provides an insight into the Fe6 core electronic structure.

Graphical abstract: Expanded redox accessibility via ligand substitution in an octahedral Fe6Br6 cluster

Supplementary files

Article information

Article type
Communication
Submitted
17 Mar 2011
Accepted
15 Apr 2011
First published
06 May 2011

Chem. Commun., 2011,47, 6344-6346

Expanded redox accessibility via ligand substitution in an octahedral Fe6Br6 cluster

T. D. Harris, Q. Zhao, R. H. Sánchez and T. A. Betley, Chem. Commun., 2011, 47, 6344 DOI: 10.1039/C1CC11561H

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